The Effect of Angiotensin Converting Enzyme Gene Polymorphism in Children with Henoch-Schonlein Purpura Nephritis
Journal of the Korean Pediatric Society
;
: 884-890, 2002.
Artículo
en Coreano
| WPRIM
| ID: wpr-152811
ABSTRACT
PURPOSE:
Henoch-Schonlein purpura(HSP) nephritis has been reported to vary from 25 to 50% among HSP patients and is a common cause of chronic glomerulonephritis in children. In our study, we evaluated the distribution and the association of the Insertion/Deletion(I/D) polymorphism of angiotensin converting enzyme(ACE) gene with clinical manifestations, particularly proteinuria in children with HSP nephritis, compared with that in HSP.METHODS:
ACE gene polymorphism was determined in children with HSP nephritis(n=33) and HSP(n=28) who were diagnosed in Busan Paik hospital from January 1996 to June 2001. The I/D polymorphism of ACE gene was determined by PCR amplication of genomic DNA.RESULTS:
The ACE I/D genotype frequency was DD 25%, ID 50%, II 25% in HSP and DD 24 %, ID 46%, II 30% in HSP nephritis, there was no significant difference in the genotype and allele frequencies between two groups. When statistical analysis was done according to the presence of D allele, the amount of 24-hour urinary protein excretion and the incidence of moderate to heavy proteinuria(>500 mg/m2/day) at onset and last follow-up were higher in DD/ID genotype than in those in II genotype, but these differences were not statistically significant.CONCLUSION:
We suggest a lack of association between I/D polymorphism of ACE gene and clinical manifestations in children with HSP nephritis. However, further follow-up studies based on a sufficient number of patients and long term follow up periods are necessary to confirm the role of I/D polymorphism of ACE gene in children with HSP nephritis.
Texto completo:
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Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Proteinuria
/
Vasculitis por IgA
/
ADN
/
Angiotensinas
/
Reacción en Cadena de la Polimerasa
/
Incidencia
/
Estudios de Seguimiento
/
Peptidil-Dipeptidasa A
/
Alelos
/
Frecuencia de los Genes
Tipo de estudio:
Estudio de incidencia
/
Estudio observacional
/
Estudio pronóstico
Límite:
Niño
/
Humanos
Idioma:
Coreano
Revista:
Journal of the Korean Pediatric Society
Año:
2002
Tipo del documento:
Artículo
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